TruVision Health LLC

Recall #F-0949-2023 · Initiated 2023-04-27

Plain-language summary

by FoodRecallsDB.info

What happened

TruVision Health LLC is recalling its TruBoost 7 Day Experience Kit because the product contains ingredients (DMHA and/or hordenine) that the FDA has determined are not safe or approved for use in dietary supplements. About 14,510 packs were distributed across the US and several other countries.

Who is at risk

Anyone who purchased and used this product should be aware of the recall, as the ingredients have not been approved for dietary supplement use.

What to do

If you have this product, stop using it and contact TruVision Health LLC or check the FDA website for return instructions. Consult your doctor if you have used this product and have any health concerns.

Product

TruBoost 7 Day Experience Kit

Reason for recall

The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.

Quantity affected

14,510 packs

Distribution

Alabama Alaska Arizona Arkansas California Colorado Connecticut Delaware Florida Georgia Hawaii Idaho Illinois Indiana Iowa Kansas Kentucky Louisiana Maine Maryland Massachusetts Michigan Minnesota Mississippi Missouri Montana Nebraska Nevada New Hampshire New Jersey New Mexico New York North Carolina North Dakota Ohio Oklahoma Oregon Pennsylvania Rhode Island South Carolina South Dakota Tennessee Texas Utah Vermont Virginia Washington West Virginia Wisconsin Wyoming and Australia, Canada, England, Germany, Ireland, New Zealand

Lot / code info

Lot 13985

Voluntary / mandated

Voluntary: Firm initiated

Initial notification

Press Release